Michael Ramcharan (Reumat Consulting Ltd) has over 30 years of experience in Quality Assurance having worked with multinational Pharmaceutical and Clinical Research Organisations (CRO) mainly in the GCP and GPV areas. He has conducted a wide variety of audits (both On-site and Remote) globally, and managed various risk-based audit programmes. He has also hosted and supported many European Regulatory Authority Inspections (eg; MHRA, EMA, Local EU country Inspectorates).
Opening remarks setting the context for Pharmacovigilance World 2026, outlining the key themes, regulatory landscape, and objectives for the conference. Setting expectations for learning, networking, and practical takeaways over two days
How leading organisations are embedding pharmacovigilance into decision-making, culture, and strategy - moving from reactive compliance to proactive patient safety.
End of Day 1 with the Chairperson's closing remarks and summarising key insights
Opening remarks outlining the focus of Day 2 on technology, data, automation, and future pharmacovigilance operating models.
A discussion on how leadership in pharmacovigilance is evolving in response to increasing data, regulatory expectations, and technological change.
End the conference with the Chairperson's closing remarks, summarizing key insights and leaving attendees with final thoughts to inspire ongoing engagement and action.
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